Department of Genetics, Evolution, Microbiology and Immunology, Institute of Biology, University of Campinas (UNICAMP), 255 Monteiro Lobato St, Campinas, São Paulo, 13083-650, Brazil.
National Laboratory of Scientific Computing (LNCC), Petropólis, Rio de Janeiro, 25651-075, Brazil.
Braz J Microbiol. 2022 Sep;53(3):1249-1262. doi: 10.1007/s42770-022-00748-8. Epub 2022 Apr 21.
Salmonella enterica causes Salmonellosis, an important infection in humans and other animals. The number of multidrug-resistant (MDR) phenotypes associated with Salmonella spp. isolates is increasing worldwide, causing public health concern. Here, we aim to characterize the antimicrobial-resistant phenotype of 789 non-typhoidal S. enterica strains isolated from human infections in the state of São Paulo, Brazil, along 20 years (2000-2019). Among the non-susceptible isolates, 31.55, 14.06, and 13.18% were resistant to aminoglycosides, tetracycline, and β-lactams, respectively. Moreover, 68 and 11 isolates were considered MDR and Extended Spectrum β-Lactamase (ESBL) producers, respectively, whereas one isolate was colistin-resistant. We selected four strains to obtain a draft of the Genome Sequence; one S. Infantis (ST32), one S. Enteritidis (ST11), one S. I 4,[5],12:i:- (ST19), and one S. Typhimurium (ST313). Among them, three presented at least one of the following antimicrobial resistance genes (AMR) linked to mobile DNA: bla, dfrA1, tetA, sul1, floR, aac(6')-laa, and qnrE1. This is the first description of the plasmid-mediated quinolone resistance (PMQR) gene qnrE1 in a clinical isolate of S. I 4,[5],12:i:-. The S. Typhimurium is a colistin-resistant isolate, but did not harbor mcr genes, but it presented mutations within the mgrB, pmrB, and pmrC regions that might be linked to the colistin-resistant phenotype. The virulence pattern of the four isolates resembled the virulence pattern of the highly pathogenic S. Typhimurium UK-1 reference strain in assays involving the in vivo Galleria mellonella model. In conclusion, most isolates studied here are susceptible, but a small percentage present an MDR or ESBL-producer and pathogenic phenotype. Sequence analyses revealed plasmid-encoded AMR genes, such as β-lactam and fluoroquinolone resistance genes, indicating that these characteristics can be potentially disseminated among other bacterial strains.
肠炎沙门氏菌引起沙门氏菌病,是人类和其他动物的一种重要感染。与沙门氏菌属分离株相关的多药耐药(MDR)表型的数量在全球范围内正在增加,引起了公众健康的关注。在这里,我们旨在描述 789 株来自巴西圣保罗州人类感染的非伤寒沙门氏菌分离株的抗微生物耐药表型,研究时间跨度为 20 年(2000-2019 年)。在非敏感性分离株中,分别有 31.55%、14.06%和 13.18%对氨基糖苷类、四环素类和β-内酰胺类耐药。此外,分别有 68 株和 11 株被认为是多药耐药和超广谱β-内酰胺酶(ESBL)生产者,而有一株对黏菌素耐药。我们选择了四株菌来获得基因组序列草图;一株肠炎沙门氏菌(ST32),一株肠炎沙门氏菌(ST11),一株 S. I 4,[5],12:i:-(ST19)和一株鼠伤寒沙门氏菌(ST313)。其中,三株菌至少携带一个与移动 DNA 相关的以下抗微生物耐药基因(AMR):bla、dfrA1、tetA、sul1、floR、aac(6')-laa 和 qnrE1。这是临床分离株 S. I 4,[5],12:i: -中首次描述质粒介导的喹诺酮类耐药(PMQR)基因 qnrE1。鼠伤寒沙门氏菌是一株黏菌素耐药分离株,但不携带 mcr 基因,但在 mgrB、pmrB 和 pmrC 区域存在突变,这可能与黏菌素耐药表型有关。这四株菌的毒力模式与高致病性鼠伤寒沙门氏菌 UK-1 参考株在体内大蜡螟模型中的毒力模式相似。总之,这里研究的大多数分离株是敏感的,但有一小部分表现出 MDR 或 ESBL 生产者和致病性表型。序列分析显示了质粒编码的 AMR 基因,如β-内酰胺类和氟喹诺酮类耐药基因,表明这些特征可能在其他细菌菌株之间传播。